HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42126349G= , CM000684.2:g.42126349G= | GRCh38 |
NC_000022.10:g.42522351G= , CM000684.1:g.42522351G= | GRCh37 |
NC_000022.9:g.40852295G= | NCBI36 |
NG_008376.3:g.8643C= | |
NG_008376.4:g.9462C= |
HGVS | Amino-acid Change | |
---|---|---|
XM_011529966.1:c.1452+267C= | XP_011528268.1:n.1452+267C= | |
XM_011529967.1:c.1452+267C= | XP_011528269.1:n.1452+267C= | |
XM_011529968.1:c.1452+267C= | XP_011528270.1:n.1452+267C= | |
XM_011529969.1:c.1308+267C= | XP_011528271.1:n.1308+267C= | |
XM_011529970.1:c.1299+267C= | XP_011528272.1:n.1299+267C= |